{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Santa Maria",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96843",
      "recalling_firm": "Hardy Diagnostics",
      "address_1": "1430 W McCoy Ln",
      "address_2": "",
      "postal_code": "93455-1005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US domestic distribution to the following states: AZ, CA, CO, FL, GA, IL, MD, ME, MI, MN, MO, NC, NE, NV, NY, PA, PR, TX, UT, VA, WI and WV.",
      "recall_number": "Z-2041-2025",
      "product_description": "HardyCHROM CRE, selective and differential culture medium for antimicrobial susceptibility testing, Product Catalog No. G323",
      "product_quantity": "4300 ea",
      "reason_for_recall": "Identified lots failed incoming quality control testing. Lots exhibited breakthrough growth of Klebsiella pneumoniae.",
      "recall_initiation_date": "20250506",
      "center_classification_date": "20250627",
      "report_date": "20250709",
      "code_info": "UDI-DI 008165760257704  G323 lot 653594P: Manufactured on March 6, 2025; Expires on May 15, 2025 G323 lot 655101P: Manufactured on April 4, 2025; Expires on June 13, 2025 G323 lot 656816P: Manufactured on April 16, 2025; Expires on June 25, 2025",
      "more_code_info": ""
    }
  ]
}